Primary carbonate/CO2 inclusions in sapphirine-bearing granulites from central Sri Lanka

High-density CO₂-rich fluid inclusions from a sapphirine-bearing granulite (Hakurutale, Sri Lanka) have been studied by microthermometry, Raman spectrometry and SEM analysis. Based on textural evidence, two groups of inclusions can be identified: primary, negative crystal shaped inclusions (group I) and pseudo-secondary inclusions, which experienced a local, limited post-trapping modification (group II). Both groups contain magnesite as a daughter mineral, occurring in a relatively constant fluid/solid inclusion volume ratio (vol_solid =0.15 total volume). CO₂ densities for group I and II differ only slightly. Both groups contain a fluid, which was initially trapped at peak metamorphic conditions as a homogeneous (CO₂+MgCO₃) mixture. Thermodynamic calculations suggest that such a fluid (CO₂+15 vol% MgCO₃) is stable under granulite facies conditions. After trapping, magnesite separated upon cooling, while the remaining CO₂ density suffered minor re-adjustments. A model isochore based on the integration of the magnesite molar volume in the CO₂ fluid passes about 1.5–2 kbar below peak metamorphic conditions. This remaining discrepancy can be explained by the possible role of a small quantity of additional water.     

Shallow-level metamorphic fluids in a high uplift rat metamorphic belt; Alpine Schist, New Zealand

Abstract Fluids, some of which are CO₂-rich (up to 40 mol.% CO₂) and some of which are highly saline (up to 18 wt% NaCl equivalent), are trapped as fluid inclusions in quartz-calcite (∼ metallic minerals) veins which cross-cut the pumpellyite-actinolite to amphibolite facies rocks of the Alpine Schist. Fluids were commonly trapped as immiscible liquid-vapour mixes in quartz and calcite showing open-space growth textures. Fluid entrapment occurred at fluid pressures near 500 bars (possibly as low as 150 bars) at temperatures ranging from 260 to 330° C. Saline fluids may have formed by partitioning of dissolved salts into an aqueous phase on segregation of immiscible fluids from a low-density CO₂-rich fluid. Calcite deposited by these fluids has δ¹³C ranging from – 8.4 to – 11.5 and δ¹⁸O from + 4 to + 13. Isotopic data, fluid compositions and mode of occurrence suggest that the fluids are derived from high-grade metamorphic rocks. Fluid interaction with wall-rock has caused biotite crystallization and/or recrystallization in some rocks and retrogression of biotite to chlorite in other rocks.
Fluid penetration through the rock is almost pervasive in many areas where permeability, probably related to Alpine Fault activity, has focussed fluids on a regional scale into fractured rocks. The fluid flow process is made possible by high uplift-rates (in excess of 10 mm/year) bringing hot rocks near to the surface.     

The amphibolite-granulite facies transition in West Uusimaa, S.W. Finland. A fluid inclusion study

This work presents the results of a fluid inclusion study of an amphibolite-granulite facies transition in West Uusimaa, S.W. Finland. Early fluid-inclusions in the granulite facies area are characteristically carbonic (CO₂), in contrast to predominantly aqueous early inclusions in the amphibolite facies area. These early inclusions can be related to peak metamorphic conditions (750-820°C and 3-5 kbar for peak granulite facies metamorphism). Relatively young CO₂ inclusions with low densities (<0.8g/cm³) indicate that the first part of the cooling history of the rocks was characterized by a near isothermal uplift.
N₂-CH₄ inclusions, with compositions ranging between pure CH₄ and pure N₂ (Raman spectral analysis), were found in the whole area. They are probably syn- or even pre-early inclusions. Only nearly critical homogenizing inclusions have been found (low density). Pressure estimates, based on densities of early fluid inclusions, show that the rapid transition of amphibolite towards granulite facies metamorphism is virtually isobaric. Granulite facies metamorphism in West Uusimaa is a thermal event, probably induced by the influx of hot, CO₂-bearing fluids.     

Fluid-mineral equilibria in prehnite-pumpellyite to greenschist facies metabasites near Flin Flon, Manitoba, Canada: implications for petrogenetic grids

A sequence of regional metamorphic isograds indicating a range from prehnite-pumpellyite to lower amphibolite facies was mapped in metabasites near Flin Flon, Manitoba. The lowest grade rocks contain prehnite + pumpellyite and are cut by younger brittle faults containing epidote + chlorite + calcite. Isobaric temperature- X _CO2 and pressure-temperature (constant X _CO2) diagrams were calculated to quantify the effects of CO₂ in the metamorphic fluid on the stability of prehnite-pumpellyite facies minerals in metabasites containing excess quartz and chlorite. Prehnite and, to a lesser extent, pumpellyite are stable only in fluids with X _co2 <0.002. For X _co2>0.002, epidote + chlorite + calcite assemblages are stable. Our calculated phase relations are consistent with regional metamorphism in the Flin Flon area in the presence of an H₂O-rich fluid and a more CO₂-rich fluid in the later fault zones. We believe that the potential effects of small amounts of CO₂ in the metamorphic fluid should be assessed when considering the pressure-temperature implications of mineral assemblages in low-grade metabasites.     

Andalusite-bearing veins at Vedrette di Ries (eastern Alps, Italy): fluid phase composition based on fluid inclusions

Abstract Andalusite-bearing veins formed during contact metamorphism in the aureole of the Vedrette di Ries tonalite. In the veins, quartz crystals that are completely armoured by andalusite or that occur in strain shadow areas contain three generations of fluid inclusions: low-salinity H₂O-CO₂-CH₄ mixtures with CH₄/(CO₂+ CH₄) ± 0.35 (type A); low-salinity aqueous fluids (type B); H₂O-free, CO₂-CH₄ fluids with the same carbonic speciation as A (type C). Carbonic types A and C typically have a dark appearance, which is attributed to graphite coatings on inclusion walls. Microstructural analysis of the host quartz and calculated densities indicate that type A inclusions were likely trapped during vein formation. These inclusions underwent strain-assisted re-equilibration during cooling that resulted in density increases without change of composition. After the rocks had cooled below about 350 ° C, type C inclusions appear to have formed from one of the immiscible fractions after unmixing of the H₂O-CO₂-CH₄ fluid mixtures. Aqueous type B inclusions, apparently trapped between 225 and 350 ° C, could represent an independent fluid, or could be the H₂O-rich fraction of unmixed type A fluids. Taking account of the uncertainties, the composition and density of the complex type A inclusion fluids are in good agreement with the properties of primary fluids calculated from the petrological data. The fluid inclusion data support the model of vein formation by hydrofracturing as a result of dehydration of graphitic metapelites. These new results also demonstrate the importance of considering strain in the interpretation of metamorphic fluid inclusions.     

Grain boundary migration of water and carbon dioxide during uplift of garnet-zone Alpine Schist, New Zealand

Abstract Deformed quartz veins in garnet-zone schist adjacent to the active Alpine Fault, New Zealand, have fluid inclusions trapped along quartz grain boundaries. Textures suggest that the inclusions formed in their present shapes during annealing of the deformed veins. Many of the inclusions are empty, but some contain carbon dioxide with densities that range from 0.16 to 0.80 g cm⁻³. No water, nitrogen or methane was detected. The inclusions are considerably more CO₂-rich than either the primary metamorphic fluid (<5% CO₂) or fluids trapped in fracture-related situations in the same, or related, rocks (<50% CO₂). Enrichment of CO₂ is inferred to have resulted from selective migration (wicking) of saline water from the inclusions along water-wet grain boundaries after cooling-induced immiscibility of a water-CO₂ mixture. Inclusion volumes changed after loss of water. Non-wetting CO₂ remained trapped in the inclusions until further percolation progressively removed CO₂ in solution. This mechanism of fluid migration dominated in ductile quartz-rich rocks near, but below, the brittle-ductile transition. At deeper levels, hydraulic fracturing is also an important mechanism for fluid migration, whereas at shallower levels advection through open fractures dominates the fluid flow regime.     

On the origin of CO2-rich fluid inclusions in migmatites

Abstract Nearly pure CO₂ fluid inclusions are abundant in migmatites although H₂O-rich fluids are predicted from the phase equilibria. Processes which may play a role in this observation include (1) the effects of decompression on melt, (2) generation of a CO₂-bearing volatile phase by the reaction graphite + quartz + biotite + plagioclase = melt + orthopyroxene + CO₂-rich vapour, (3) selective leakage of H₂O from CO₂+ H₂O inclusions when the pressure in the inclusion exceeds the confining pressure during decompression, and (4) enrichment of grain-boundary vapour in CO₂ by subsolidus retrograde hydration reactions.     

Experimental diffusion of hydrogen into synthetic fluid inclusions in quartz

Abstract Quartz-hosted, synthetic CO₂-H₂O fluid inclusions behave as open systems with respect to diffusional transfer of hydrogen during laboratory-simulated metamorphic re-equilibration at 650, 750 and 825°C and 1.5 kbar total pressure with f_O2 defined by the C-CH₄ buffer. Microthermometry and Raman spectroscopy show that the initial CO₂-H₂O inclusions become CO₂-CH₄-H₂-H_2O
inclusions after diffusive influx of hydrogen from the reducing confining medium. Measurable changes are observed in inclusion compositions after only 15 days of re-equilibration, implying significant hydrogen mobility at still lower temperatures over geological time spans. Results of synthetic inclusion re-equilibrium experiments have profound implications for the interpretation of natural fluid-inclusion data; failure to account for potential hydrogen migration in inclusions from high-temperature geological environments may lead to erroneous estimates of P-T, and/or the compositions of metamorphic fluids.     

Gas Measurement of Fluid Inclusions from the Hishikari Epithermal Gold Deposit, Southern Kyushu, Japan, Using Laser Raman Microprobe

Abstract. Laser Raman microprobe analysis was performed on the fluid inclusions from the Honko-Sanjin zone in the Hishikari epithermal gold deposit, southern Kyushu, Japan. Gas concentrations of fluid inclusions through the zone were below detection limits (e.g., 5 mmole/kg H₂O for CO₂), with an exception at shallow portion in which the CO₂/N₂ mole ratio was determined to be 5.3. Boiling of hydrothermal solutions probably separated gases from ore fluids at the deep portion of the deposit, and migration of gases to shallow portion resulted in CO₂-rich steam-heated water and related acid alteration.     

High-density early CO2 fluids in the ultrahigh-temperature granulites of Ihouhaouene (In Ouzzal, Algeria)

Fluid inclusion studies in rocks from the Lower Proterozoic granulites from western Hoggar (Algeria) provide new evidence for the hypothesis that a CO₂-rich, H₂O-poor fluid was present during the high-grade metamorphism. CO₂ inclusions represent the main fluid trapped in the Ihouhaouene ultrahigh-temperature (over 1000 °C) and high-pressure (10 to 14 kbar) granulites. The microthermometric and Raman microspectrometric measurements indicate that the carbonic fluid is mainly composed of CO₂ with minor amounts of CH₄ and N₂ detected in some inclusions (< 4 mol% CH₄). Carbonic fluid densities range from 1.18 to 0.57 g/cm³. The highest densities are recorded in superdense carbonic inclusions presenting evidence of the earliest trapping and they correspond to the fluid densities expected for the P–T conditions of the peak of metamorphism in the area previously determined from mineral geothermobarometers. Lower densities of carbonic fluids mainly result from the reequilibration of earlier trapped fluid inclusions during retrograde metamorphism and final uplift of the metamorphic terrane, but a new influx of carbonic fluids during the retrograde event remains possible. Carbonic fluids can be produced in situ from decarbonation reactions in interlayered impure marbles during the prograde event or derived from CO₂ flushing from underlying basic intrusions. The aqueous fluids present large variations of composition (0.5 to 30 wt.% NaCl equivalent) and densities (1.16 to 0.57 g/cm³). They clearly correspond to post-metamorphic fluids because they mainly occur along microfractures, they do not show any evidence of immiscibility with the carbonic fluids and mixed aquo-carbonic inclusions have not been observed. The percolation of aqueous fluids is related to the Pan-African tectonometamorphic event.     

Genesis of Kanggur Gold Deposit in Eastern Tianshan Orogenic Belt, NW China: Fluid Inclusion and Oxygen and Hydrogen Isotope Constraints

Abstract. Primary fluid inclusions in quartz and carbonates from the Kanggur gold deposit are dominated by aqueous inclusions, with subsidiary CO₂-H₂O inclusions that have a constant range in CO₂ content (10–20 vol %). Microthermometric results indicate that total homogenization temperatures have a wide but similar range for both aqueous inclusions (120 to 310C) and CO₂-H₂O inclusions (140 to 340C). Estimates of fluid salinity for CO₂-H₂O inclusions are quite restricted (5.9∼10.3 equiv. wt% NaCl), whereas aqueous inclusions show much wider salinity ranging from 2.2 to 15.6 equivalent wt %NaCl.
The 6D values of fluid inclusions in carbonates vary from -45 to -61 %, in well accord with the published δD values of fluid inclusions in quartz (-46 to -66 %). Most of the δ¹⁸O and δD values of the ore-forming fluids can be achieved by exchanged meteoric water after isotopic equilibration with wall rock by fluid/rock interaction at a low water/rock ratio. However, the exchanged meteoric water alone cannot explain the full range of δ¹⁸O and δD values, magmatic and/or meta-morphic water should also be involved. The wide salinity in aqueous inclusions may also result from mixing of meteoric water and magmatic and/or metamorphic water.     

P–T conditions for the Arendal granulites, southern Norway: implications for the roles of P, T and CO2 in deep crustal LILE-depletion

Abstract The orthopyroxene-clinopyroxene, garnet-orthopyroxene and garnet-clinopyroxene geothermometers, and the garnet-orthopyroxene-plagioclase, garnet-clinopyroxene-plagioclase and anorthite-ferrosilite-grossular-almandine-quartz geobarometers are applied to metabasites and the garnetplagioclase-sillimanite-quartz geobarometer is applied to a metapelite from the Proterozoic Arendal granulite terrain, Bamble sector, Norway. P–T conditions of metamorphism were 7.3 ± 0.5 kbar and 800 ± 60°C.
This terrain shows a regional gradation from the amphibolite facies, into normal LILE content granulite facies rocks and finally strongly LILE deficient granulite facies gneisses. Neither P nor T vary significantly across the entire transition zone. The change in 'grade'parallels the increasing dominance of CO₂ over H₂O in the fluid phase.
LILE-depletion is not a pre-condition of granulite facies metamorphism: granulites may have either 'depleted'or 'normal'chemistries. The results presented herein show that LILE-deficiency in granulite facies orthogneisses is not necessarily related to variations in either P or T . The important mechanisms in the Arendal terrain were (a) direct synmetamorphic crystallization from magma, with primary LILE-poor mineralogies imposed by the prevailing fluid regime, and (b) metamorphic depletion, involving scavenging of LILEs during flushing by mantle-derived CO₂-rich fluids. The latter process is constrained by U–Pb and Rb–Sr isotopic work to have occurred no later than 50 Ma after intrusion of the acid-intermediate gneisses, and was probably associated with contemporary basic magmatism in a tectonic environment similar to a present day cordilleran continental margin.     

Syndeformational fluid trapping in quartz: determining the pressure-temperature conditions of deformation from fluid inclusions and the formation of pure CO2 fluid inclusions during grain-boundary migration

Abstract Observations and microthermometric data on fluid inclusions from a terrane that underwent deformation following peak metamorphic conditions show that grain-boundary migration recrystallization favours the entrapment of carbonic inclusions whereas microfracturing during brittle deformation favours the infiltration and eventual entrapment of aqueous fluids. Our results imply that pure CO₂ fluid inclusions in metamorphic rocks are likely to be the residue of deformation-recrystallization process rather than representing a primary metamorphic fluid.
Where the temperature of deformation can be deduced by other means, the densities of fluid inclusions trapped during recrystallization, which we call recrystallization-primary fluid inclusions, can be used to constrain the ambient pressure during deformation. Using these constraints, the data imply that the post-metamorphic Hercynian exhumation in Sardinia brought rocks at 300° C to within 3km of the surface. This conclusion is similar to that described for the rapidly uplifted Southern Alps in New Zealand.     

Synthetic Fluid Inclusions in the Systems NaCl-H2O and NaCl-CO2-H2O: Dissolution Temperatures of Halite

Abstract. This study examined the effect of CO₂ on NaCl solubility in hydrothermal fluid, with the synthetic fluid inclusion technique. Fluid inclusions of 30–40 wt% NaCl and 5 mol % CO₂ were synthesized, and their halite dissolution temperatures, T_m(halite), were measured. The solubilities of NaCl in CO₂-bearing aqueous fluid were obtained at 160–320C under vapor-saturated pressures. The T_m(halite) value in aqueous fluid with 5 mol % CO₂ obtained in this study agrees with that of Schmidt et al. (1995), showing that 5 mol % CO₂ reduces the solubility of NaCl by about 1 wt%.
Calculation of magnetite solubility suggests that 5–10 mol % CO2 decreases magnetite solubility by 4.5–8.9 % relative to the magnetite solubility in CO2-free solution. Therefore, an increase of CO2 content in ore-forming solutions may cause deposition of iron minerals and produce ore deposits.     

Microthermometric Evidence for the Formation of Ca-rich Hypersaline Brine and CO2–rich Fluid in the Mori Geothermal Reservoir, Japan

Abstract: Fluid inclusions in hydrothermal quartz and anhydrite samples from the Mori geothermal field, southwest Hokkaido, have been studied microthermometrically using heating/freezing stages. Based on homogenization temperatures of fluid inclusions, salinities after correction of effect of freezing-point depression of CO₂ on ice melting temperatures of fluid inclusions, and previous geochemical data by Yoshida (1991), we discuss the geneses of various types of inclusion fluids in the Mori geothermal reservoir.     

小秦岭大湖金钼矿床地质特征及成矿流体

小秦岭地区位于华北克拉通南缘,赋存许多大型-超大型的金矿床,大湖金钼矿床位于小秦岭北矿带。大湖金钼矿床成矿具有多期多阶段特点,包括热液期和表生期,根据矿脉穿切关系、矿石的矿物组成以及结构、构造研究,热液期分为4个成矿阶段,即石英-钾长石-辉钼矿阶段(Ⅰ)、石英-黄铁矿-自然金阶段(Ⅱ)、石英-多金属硫化物-自然金阶段(Ⅲ)和石英-碳酸盐阶段(Ⅳ)。流体包裹体岩相学、激光拉曼成分分析和冷热台测温结果表明,大湖金钼矿的初始成矿流体属H₂O-CO₂-NaCl体系,包裹体分为三种类型,即CO₂-H₂O型包裹体(C型)、水溶液型包裹体(W型)和纯CO₂型包裹体(PC型)。成矿Ⅰ、Ⅱ、Ⅲ和Ⅳ阶段包裹体均一温度范围分别为275.3~350.0 ℃、260.0~312.7 ℃、245.3~287.6 ℃和237~251 ℃,流体盐度范围为5.2%~16.7%,密度为0.777~1.108 g/cm³,为中-高温、中-低盐度、低密度流体,与变质流体特征一致。均一温度从Ⅰ阶段→Ⅳ阶段呈逐渐下降趋势,盐度从Ⅰ阶段→Ⅲ阶段逐渐降低,Ⅳ阶段沸腾作用使流体中的气体组分逸出,导致剩余流体的浓缩盐度增高。流体成矿压力范围为58.0~196.3 MPa,对应成矿深度范围为3.0~7.1 km。矿区普遍存在的围岩蚀变表明水岩反应强烈,氢同位素δD为-90‰~-44‰,成矿流体氧同位素δ¹⁸O_水范围为2.1‰~5.9‰,属于变质热液范围;在δ¹⁸O_水-δD组成图解投图中落在变质水范围左下侧,Ⅱ、Ⅲ阶段样品的δ¹⁸O_水较Ⅰ阶段整体左移,表明高温变质流体与围岩(斜长角闪岩等变质岩)发生水岩反应,导致同位素互换平衡。大湖金钼矿床受区域近东西向断裂构造控制,属典型的断控脉状矿床,成矿流体以变质水为主,矿床主要特征与典型的造山型金矿特征相符。     

Stable isotopic and fluid inclusion evidence for meteoric fluid penetration into an active mountain belt; Alpine Schist, New Zealand

Calcite and quartz veins have formed, and are forming, in steeply dipping fissures in the actively rising Alpine Schist metamorphic belt of New Zealand. The fluids that deposited these minerals were mostly under hydrostatic pressure almost down to the brittle-ductile transition, which has been raised to 5-6 km depth by rapid uplift. Some fluids were trapped under lithostatic pressures. Fluids in the fissure veins were immiscible H₂O + NaCl-CO₂ mixtures at 200-350 C. Bulk fluid composition is 15-20 mol% CO₂ and <4.3 total mol CH₄+ N₂+ Ar/100mol H₂O. Water hydrogen isotopic ratio δD_H2O in the fissure veins spans -29 to -68‰, δ¹⁸O_H2O -0.7 to 8.5‰, and bulk carbon isotopic ratio δ¹³C ranges from -3.7 to -11.7‰. The oxygen and hydrogen isotopic data suggest that the water has a predominantly meteoric source, and has undergone an oxygen isotope shift as a result of interaction with the host metamorphic rock. Similar fluids were present during cooling and uplift. Dissolved carbon is not wholly derived from residual metamorphic fluids; part may be generated by oxidation of graphite.     

Dehydration reaction and isotope front transport induced by CO2 infiltration at Nuliyam, South India

The field relations from a quarry at Nuliyam, South India, illustrate dehydration of an amphibolite facies gneiss to granulite facies charnockite by CO₂ influx, over a scale of 30 m. Both the calc-silicate source of the fluids and the full extent of their penetration into the gneiss are preserved in a continuous section. Fluid flow is by a hydraulic fracture mechanism, but is thought to be pervasive. The sharp reaction front predicted by the continuum mechanical theory for advective fluid transport is not observed. The front spreading is on too large a scale for either diffusive or dispersive control and is due to local kinetic disequilibrium between the fluid and rock, although the divariant nature of the reaction may also have a limited effect. The time-integrated fluid flux varies from the instantaneous porosity at the fluid front to 20 vol. % adjacent to the calc-silicate. Carbon isotope budgets suggest that decarbonation of the calc-silicate by a Rayleigh fractionation process provides a sufficient source for the CO₂ influxing into the gneiss. Graphite abundances vary from 0.01 to 0.1% (by weight), it is principally derived by precipitation from the fluid and may be modelled from phase equilibria. Carbon isotope fronts coincide with the reaction front on the scale of sampling, although isotopic disequilibrium between graphite and inclusion-CO₂ also implies local fluid-rock disequilibrium.     

Magmatic and hydrothermal processes in the Bouvet Triple Junction Region (South Atlantic)

Results of electron microprobe and microthermometric studies of samples collected from the Bouvet Triple Junction Region (BTJR) during a joint Russian-Italian geological expedition on the R/V Academician Nikolaj Strakhov (1994) have revealed new data on the composition of basaltic magmas and oceanic hydrothermal fluids connected with magmatic processes. Detailed analysis of basaltic glasses shows that the modem Mid-Atlantic Ridge (MAR) rift valley is composed of normal mid-ocean ridge basalts with low concentrations of K₂ O and TiO_z (N-MORB), while its flanks are more enriched with these components approaching E-MORB. A marked influence of the Bouvet hot spot volcanism on magma generation on the South-West Indian Ridge (SWIR) near Bouvet Island is observed. Basaltic melts in this area belong to alkalic and transitional series and have maximum contents of K₂O, TiO₂, H₂O.
Microthermometric analyses of fluid inclusions in the samples from the BTJR have revealed major differences in the oceanic hydrothermal fluid systems on the MAR and near SWIR, which depends on the peculiarities of magma. In the area of the MAR (with dry melts) only H₂O solution inclusions in quartz were found; thus, seawater is probably the only primary source of hydrothermal fluids (NaCl + MgCl₂+ H₂O; T = 170–200°C). In the SWIR area (with the high content of water in melts) syngenetic liquid CO₂ and H₂O solution inclusions in quartz indicate the influence of the magmatic fluid component on the ore-forming water/carbon dioxide solutions (NaCl + CaC1₂+ H₂O + CO₂; T = 200–310 °C; P = 900–1700 bar).     

Ijolite versus carbonatite as sources of fenitization

Ijolite-carbonatite complexes are ubiquitously surrounded of an aureole of metasomatically altered rocks. The process of alteration is termed fenitization and is generally caused by peralkaline fluids emanating from cooling alkaline, i.e. ijolite and carbonatite magmas. Ijolites and carbonatites normally occur together and attempts to determine the source of the fenitizing fluids may therefore lead to controversial, if not erroneous, conclusions.
Mineralogical and chemical data of fenites from Oldoinyo Lengai (Tanzania), Fen (Norway), and Alnö (Sweden) are reviewed in the present paper in order to reveal the main factors controlling the fenitization around ijolite and carbonatite. Despite the overall alkaline nature of the process, variables such as XCO₂ of the fluid, activity gradients of SiO₂, Al₂O₃ and CaO, FeO/MgO ratio, f O₂ and temperature gradients may differ, producing distinctive patterns of fenitization around the two magmatic sources. The ijolitic-type fluid has low XCO₂, high activities of alkalies, SiO₂ and Al₂O₃, and low activity of CaO. The f O₂ evolves along the hm-mt buffer conditions and the temperature falls gradually with distance from the magmatic source. The carbonatitic-type fluid has high XCO₂, high activities of alkalies and CaO, and low activities of SiO₂ and Al₂O₃. Temperatures and f O₂ are initially high, but decrease sharply with distance from the source. Moreover, the CO₂-rich fluid may complex and transport the REE.